Reply: Mutations inTUBB4Aand spastic paraplegia-Reference-Cited by-同舟云学术

Reply: Mutations inTUBB4Aand spastic paraplegia

Published:2015-10-19 Issue:13 Volume:30 Page:1858-1859
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Chamova Teodora¹,Kancheva Dahlia²³⁴,Guergueltcheva Velina⁵,Mitev Vanio⁴,Azmanov Dimitar N.⁶⁷,Kalaydjieva Luba⁷,Jordanova Albena²³⁴,Tournev Ivailo¹⁸

Affiliation:

1. Medical University of Sofia, Faculty of Medicine, Department of Neurology, Clinic of Neurology; University Hospital Alexandrovska; Sofia Bulgaria

2. Molecular Neurogenomics Group, Department of Molecular Genetics; Antwerp Belgium

3. Neurogenetics Laboratory, Institute Born-Bunge; University of Antwerp; Antwerp Belgium

4. Department of Medical Chemistry and Biochemistry, Molecular Medicine Center; Medical University-Sofia; Sofia Bulgaria

5. Department of Neurology; Sofiamed Hospital; Sofia Bulgaria

6. Department of Diagnostic Genomics, PathWest; QEII Medical Centre; Nedlands WA Australia

7. Harry Perkins Institute of Medical Research and Centre for Medical Research; The University of Western Australia; Perth Australia

8. Department of Cognitive Science and Psychology; New Bulgarian University; Sofia Bulgaria

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference17 articles.

1. Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia;Kancheva;Mov Disord,2015

2. Mutations in TUBB4A and spastic paraplegia;Kumar;Mov Disord

3. Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene;Blumkin;Neurogenetics,2014

4. Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC);Ferreira;Am J Med Genet,2014

5. Expanding the phenotypic spectrum of TUBB4A-associated hypomyelinating leukoencephalopathies;Miyatake;Neurology,2014